ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.489A>G (p.Ala163=)

gnomAD frequency: 0.00001  dbSNP: rs201815341
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001425982 SCV001628623 likely benign Cowden syndrome 2020-08-02 criteria provided, single submitter clinical testing
Ambry Genetics RCV002329470 SCV002634556 likely benign Inborn genetic diseases 2021-01-21 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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